- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06406738
Simulator Use in Newborn First Care
The Effect of High Reality Simulator Use in Newborn First Care Training on the Knowledge, Skills, Satisfaction and Self-Confidence of Midwifery Students
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hypotheses H01: There will no difference between the students' knowledge skills, satisfaction, and self-confidence of the simulation-based newborn first care training group and the knowledge skills, satisfaction, and self-confidence score of control group.
The study will be carried out in two different groups. The practice will start with meeting the students who apply to the study. After the students are evaluated in terms of eligibility criteria for the research, the students who are eligible will be informed about the research and written informed consent will be obtained from the women who accept. The random distribution of women to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups.
Newborn first care training will be given by the responsible investigator, and then one of the groups separated by randomization will perform newborn first care on the second group model using High Reality Simulator. These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Samsun
-
Ilkadim, Samsun, Turkey, 55100
- Sumeyye
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Agreeing to participate in the research and obtaining written permission,
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: High Reality Simulator
Newborn first-care training will be given by the responsible investigator, and then one of the groups will be allocated by randomization.
Using High Reality Simulator will perform Newborn first-care.
These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one.
|
Using High Reality Simulator will perform newborn first-care.
Other Names:
|
|
No Intervention: control group
Using model will perform Newborn first-care.
These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
First Care of the Newborn Information Form
Time Frame: immediately before simulation and immediately after the training and 6 weeks later
|
t is a material developed by Karaçam Z, Çoban A, Taşpınar A (2018), consisting of 25 questions, to measure the student's knowledge level about newborn care.
the minimum score is 0 and maximum score is 75.
|
immediately before simulation and immediately after the training and 6 weeks later
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Sümeyye BAL, Ph.D., Ondokuz Mayıs University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2023/3
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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